Hughes Syndrome Foundation

A UK registered charity dedicated to promoting awareness and funding research into Hughes Syndrome which is also known medically as the antiphospholipid syndrome (APS). Our website provides information about the charity and all aspects of Hughes Syndrome for patients, doctors and supporters.

ITPeducation.com™

ITPeducation.com™ is part of an educational curriculum incorporating a series of activities. It is designed to provide evidence-based clinical information on the diagnosis and management of patients with ITP to hematologists, oncologists, and other health care professionals. The Web site houses online educational activities including interactive patient cases, peer-to-peer dialogue, slide catalogues, and primers. Other educational activities include regional case-exchange meetings; national Grand Rounds; national & regional symposia; and 2 printed educational primers.

Scleroderma Foundation

The Scleroderma Foundation is the leading non-profit supporter of scleroderma research in the United States. To promote education of the disease, the foundation facilitates health and professional seminars, produces and distributes literature and conducts publicity campaigns, as well as offering peer counseling, mutual support programs, and physician referrals.